CC1=CC=C(C=C1)S(=O)(=O)N1CCC(CC1)C(=O)N\N=C\C1=CC=CC=C1[N+]([O-])=O

InChIKey=JEHUKRZPCUGJIG-KGENOOAVSA-N

C20H22N4O5S

430.48

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Piperidinecarboxamides Benzenesulfonyl compounds Nitrobenzenes Nitroaromatic compounds Organosulfonamides Sulfonyls Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Carboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Carbonyl compounds Organic salts Organic zwitterions Organonitrogen compounds

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Nitrobenzene - Piperidinecarboxamide - Benzenesulfonyl group - Nitroaromatic compound - Piperidine - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - C-nitro compound - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Organic oxoazanium - Organic zwitterion - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organic salt - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as n,n-disubstituted p-toluenesulfonamides. These are p-toluenesulfonamide derivatives in which the sulfonamide moiety is N,N-disubstituted.

Not available